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Completed

NCT Number: NCT03222206

The Comparison of Effect Between Salsalate and Placebo in Osteoarthritis With Nonalcoholic Fatty Liver Disease

This Study purpose to verify change of variety factors that the cause of nonalcoholic fatty liver disease and its process through salsalate injection to osteoarthritis patient who has non alcoholic fatty liver

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Korea University Guro Hospital

Seoul, 08308, South Korea

About this study

Salsalate, the salicylic acid dimer that is one of anti-inflammatory and kind of salicylate. Aspirin(Acetylated salicylic) is known as nonsteroidal anti-inflammatory, also salsalate is widely used painkiller and anti-inflammatory without prescription in Europe and America through the long time and it was approved as osteoarthritis and rheumarthritis treatment in Korea. Especially salsalate is switched to salicylic acid(active metabolite) 15% rate lower than the same dose of aspirin (3.5g vs. 5g).

Salsalate is cyclooxygenase antagonist, it make anti-inflammatory effect by hinder creation of variety inflammatory induction factors like interleukin-6, Tumor Necrosis Factor (TNF)-alpha, C-reactive protein. This anti-inflammatory reaction is known to block Nuclear Factor(NF)-kappaB gene action by hinder action of IkappaB kinase. Also salsalate was reported it has positive effect to gluco metabolism as performed role of insulin-sensitizing. Therefore, the above mechanism of salsalate was expected that it can be had positive effect to metabolic disease like diabetes and obesity, and related studies are performed considerably at present.

There is no clinical trial for non alcoholic fatty acid related salsalate, and there was the animal study result that salsalate may reduce occurence of non alcoholic fatty acid and fibrosis by hinder non alcoholic fatty acid creation and inflammation mediation path.

Therefore, this Study purpose to verify change of variety factors that the cause of nonalcoholic fatty liver disease and its process through salsalate injection to osteoarthritis patient who has non alcoholic fatty liver

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Osteoarthritis patient who has non alcoholic fatty liver
  • Standard of non alcoholic fatty liver diagnosis
  • Fatty liver on abdominal ultrasonography
  • Patient who has no evidence as hepatitis B, hepatitis C, immune hepatitis, metabolic hepatitis and other chronic hepatitis
  • Osteoarthritis patient who has never been treated

Exclusion criteria

  • Unsuitable on inclusion criteria
  • Thiazolidinedione injected patient for diabetes treatment or patient who has changed injected drug last 6 month
  • Patient who is treating nonsteroidal antiinflammatory drugs for osteoarthritis
  • Renal dysfunction : serum creatinine level 1.5mg/dl or creatinine clearance < 60ml/min
  • Anamnesis of gastrointestinal tract bleeding
  • Upper 5 times(200IU/l) the normality of Aspartate Transaminase(AST), Alanine Transaminase(ALT)
  • Pregnant or Breastfeeding
  • Patient who has untreated malignant tumor
  • Liver transplantation patient
  • Patient who has liver function Child-Pugh B over
  • Patient who has serious disease that was estimated influence to study (e.g. Congestive heart failure, Kidney failure, Chronic pancreatitis, Malignant tumor)
  • Patients who has been injected immunomodulatory and immunosuppressant(inclusive universal corticosteroids) before 6 month enrollment or at present
  • Patient who was judged unsuitable for study by investigator

Treatment and study plan

Salsalate

Drug
  • Medicate salsalate 2g/day after run-in period
  • Check side effect after 1 month and Control dosage (2g/day or 3g/day)
  • Check side effect after 2 month

Other names: A03850041

Placebo

Other
  • Medicate placebo 2g/day after run-in period
  • Check side effect after 1 month and Control dosage (2g/day or 3g/day)
  • Check side effect after 2 month

Primary outcomes

  1. Change of controlled attenuation parameter

    Time frame: baseline and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  2. Change of hepatokine as Fetuin-A

    Time frame: baseline and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  3. Change of pulse wave velocity

    Time frame: baseline and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  4. Change of adipokine as Adiponectin

    Time frame: baseline and 8weeks

    Estimation of salsalate single injection group and placebo injection group

Secondary outcomes

  1. Change of controlled attenuation parameter

    Time frame: baseline and 4weeks

    Estimation of salsalate single injection group and placebo injection group

  2. Change of hepatokine as Fetuin-A

    Time frame: baseline and 4weeks

    Estimation of salsalate single injection group and placebo injection group

  3. Change of pulse wave velocity

    Time frame: baseline and 4weeks

    Estimation of salsalate single injection group and placebo injection group

  4. Change of adipokine as Adiponectin

    Time frame: baseline and 4weeks

    Estimation of salsalate single injection group and placebo injection group

  5. Numerical value change of fatty liver index

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  6. Numerical value change of hepatic fibrosis as Nonalcoholic Fatty Liver Disease(NAFLD) fibrosis score

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  7. Change of saccharometabolic factors as Homeostasis Model Assessment(HOMA)-Insulin Resistance(IR), Homeostasis Model Assessment(HOMA)-B, Fasting glucose, Insulin, C-peptide, HbA1c, Glycated albumin

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  8. Change of lipid metabolic factors as Cholesterol, Triglyceride, LDL-cholesterol HDL-cholesterol and liver function test as Aspartate Transaminase(AST) and Alanine Transaminase(ALT)

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  9. Change of inflammatory factors as C Reactive Protein(CRP), Tumor Necrosis Factor(TNF)-a

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  10. Change of liver fibrosis factors as hyaluronic acid

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  11. Change of symptom of osteoarthritis as visual analog score for pain

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  12. Change of function of osteoarthritis as WOMAC (The Western Ontario and McMaster Universities Osteoarthritis Index)

    Time frame: baseline, 4weeks and 8weeks

    Estimation of salsalate single injection group and placebo injection group

  13. Stability comparison like side effect

    Time frame: Up to 2month

    Estimation with treatment-related adverse events as assessed by CTCAE v4.0

Sponsors and collaborators

Lead sponsor

Korea University Guro Hospital

Other

Collaborators

  • Kuhnil Pharmaceutical Co., Ltd.

Registry information

Official study title

The Comparison of Effect Between Salsalate and Placebo in Osteoarthritis With Nonalcoholic Fatty Liver Disease: Investigator Initiated Randomized Placebo-controlled Double-blind, Pilot Study

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 19, 2017
Registry last updated
Aug 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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